Unraveling Regulatory Challenges in Transitioning from Pre-Clinical to Clinical Phases, Focusing on the IND Process
Time: 1:01 pm
day: Pre-Conference Workshop Day
Details:
Cell and gene therapies span pipelines across every phase of development, from preclinical stages through to approval. This presents an opportunity to learn from various phases and make regulatory processes more efficient.
Join this session to:
- Map out the regulatory landmarks from pre-clinical to clinical phases to gain a highlevel viewpoint of potential bottlenecks
- Focus on IND submissions to map out the key stages of the submission process
- Hear case studies from companies overcoming challenges in transitioning between development stages to review and apply learnings to your own work
- Reflect on future collaboration opportunities to brainstorm possible solutions
